Fei Ye

Purpose: To investigate the effects of pleomorphic adenoma gene like-2 (PLAGL2) on oral squamous cell carcinoma (OSCC). Methods: The effects of PLAGL2 on OSCC (CAL-27 and HSC-3) were conducted with loss- and gain-functional assays. Cell proliferation was determined by Cell Counting Kit-8 (CCK8) and colony formation assays. Cell metastasis was assessed by Transwell and wound healing assays. Cell apoptosis of cisplatin-resistant OSCC was evaluated by flow cytometry. Results: PLAGL2 expression was significantly elevated in OSCC (p < 0.001), while silencing of PLAGL2 significantly reduced cell proliferation and metastasis of OSCC (p < 0.001). However, overexpression of PLAGL2 promoted OSCC progression through increase in cell proliferation, invasion, and migration. Knockdown of PLAGL2 promoted cell apoptosis of -resistant OSCC, but significantly downregulated protein expression of programmed cell death ligand 1(PD-L1) and zinc finger E-box-binding homeobox 1 (ZEB1) in OSCC (p < 0.01). Moreover, loss of ZEB1 attenuated the PLAGL2 overexpression-induced increase in ZEB1 and PD-L1. Loss of PLAGL2 also reduced in vivo tumor growth of OSCC via regulation of cluster of differentiation 4 protein (CD4) and CD8. Conclusion: Knockdown of PLAGL2 exerts anti-tumor effects, improves cisplatin resistance, and enhances anti-tumor immunity in OSCC through suppression of ZEB1/PD-L1 pathway. Thus, PLAGL2 might be a potential therapeutic target for the treatment of OSCC.

To develop the state‐of‐the‐art polymer membrane fuel cells. Both maximization of oxygen reduction reaction (ORR) activity on Pt cathode and minimization of Pt content in the cathode are required. For this challenge, the defect interface on oxide support was modified by proton beam irradiation method. Pt‐CeO _x nanowire/C (Pt/C = 0.02) was fabricated using the proton beam irradiation method. Since the radical density generated by proton beam irradiation is two orders of magnitude greater than that of electron beam irradiation, the CeO _x nanowire surface was fully converted to a thin layer of Pt‐O‐Ce bonds under proton beam irradiation. The ORR activity observed for fabricated sample with above active surface layer was higher than that of conventional Pt/C (Pt/C = 0.2) and comparable to that of Pt‐CeO _x nanowire/C (Pt/C = 0.2) fabricated by conventional methods. From the combination of microanalysis characterization and surface atomistic simulation, we concluded that the Pt‐O‐Ce bond was formed on defect‐rich regions of the CeO _x nanowire and this leads to a maximized ORR activity on the fabricated sample. Based on all experimental data, it is concluded that the surface modification of CeO _x nanowire support using proton beam irradiation is useful for a lowering the Pt content of the cathode with high ORR activity.

Invited for this month's cover is the group of Prof. Dr. Toshiyuki Mori at National Institute for Materials Science (NIMS), Japan. The front cover picture shows the formation of new active sites on Ni in the anode of a solid oxide fuel cell (SOFC), which displays high performance at intermediate temperature. The combination of processing route design, microanalysis, and surface atomistic simulation provides us with a new design paradigm for fabrication of high‐performance SOFCs. Read the full text of the article at 10.1002/cplu.201800170.

In recent years, the lowering of the operation temperature of solid oxide fuel cells (SOFCs) has attracted much attention owing to the trade‐off between the best performance and the life span of SOFCs. For this challenge, new active sites on the Ni surfaces in a Nickel–Yttria‐Stabilized Zirconia (Ni‐YSZ) cermet anode of SOFCs have been created by deposition of trace amounts of platinum oxide (PtO_x) followed by an activation step of the anode at 1073 K in a hydrogen flow. The internal resistance (IR) free value (185 mA cm⁻² at 0.8 V) observed for the single cell with an anode sputtered with a trace amount of PtO_x (Pt content in anode: from 9 to 91 ppm) at 973 K is conspicuously higher than that of a similar single cell with a nonsputtered cermet anode (85 mA cm⁻²) at 0.8 V and 1073 K. Transmission electron microscopy microanalysis shows that the defect structure is formed on a partially oxidized Ni surface by active Pt species. Also, surface atomistic simulation on NiO (111) predicts the formation of Frenkel defect clusters with Pt cations, which partially cover the Ni surface. The formation of Frenkel defect clusters on the partially oxidized Ni surface (i.e., creation of new active sites for formation of water molecules) promotes the anode reaction, resulting in improvements in the anode performance of SOFC single cells at 973 K. Design of the aforementioned new active sites on Ni through sputtering of trace amounts of PtO_x provides a great opportunity for “radical innovation” in the design of intermediate‐temperature SOFCs.